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Anmuth Medical International

FDA UDI

Class I (US FDA UDI)

by Anmuth Medical International Llc

Identity

Trade Name
Anmuth Medical International FDA UDI
Generic Name
Orthopaedic implantable-device cutter FDA UDI
Device Name
Pin Cutter, Side Cutting, Stainless, 1/4" (6.3mm) max cutting capacity, 56cm/22" FDA UDI
Model / Reference
39-546-54TC FDA UDI
Description
Pin Cutter, Side Cutting, Stainless, 1/4" (6.3mm) max cutting capacity, 56cm/22" FDA UDI

Identifiers

Catalog Number
39-546-54TC FDA UDI
Primary DI / UDI-DI
08403207010162 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Orthopaedic implantable-device cutter FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 0.25 Inch FDA UDI

Category: Orthopaedic implantable-device cutter

Anmuth Medical International by Anmuth Medical International Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic implantable-device cutter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2deb20a4-b872-439c-bbf9-a1204953681d 36 fields · synced May 30, 2026